Event Group
Event Groups are part of the Adverse Events Module within the Results Section. They provide a way to organize and summarize adverse event data by grouping related events together.
Each Event Group typically represents a category or class of adverse events and includes statistical information such as the number of participants affected and at risk for different event types: deaths, serious events, and other events.
Event Group path is as follows:
Study -> Results Section -> Adverse Events Module -> Event Group
Event Group
Ignite Creation Date:
2025-12-24 @ 4:58 PM
Ignite Modification Date:
2025-12-25 @ 2:39 PM
NCT ID:
NCT03032250
Group ID:
EG001
Title:
Group II Control Group
Description:
Caregivers received standard of care throughout course of intervention, with option to receive study intervention at end of study.
Watch video: Watch video on a DVD
Module completion of the Prepare to Care kit: Complete modules of the Prepare to Care kit
Quality-of-Life Assessment: Ancillary studies
Survey Administration: Ancillary studies
Salivary cortisol collection: Obtained at three times a day (at awakening, 30 minutes post awakening and bedtime) for two consecutive days for eligible caregivers in both groups. Samples collected by placing a cotton ball under the tongue for approximately 1-2 minutes which is subsequently stored in a plastic tube and refrigerated.
Deaths Number Affected:
0
Deaths Number At Risk:
None
Serious Number Affected:
0
Serious Number At Risk:
18
Other Number Affected:
0
Other Number At Risk:
18
Study:
NCT03032250
Results Section:
NCT03032250
Adverse Events Module:
NCT03032250